Clinical Monitoring Specialist

1 semana atrás


Lisboa, Lisboa, Portugal Phiture Tempo inteiro

At Phiture, we're revolutionizing the development process by ensuring the swift delivery of life-changing ideas and therapies to patients in need. Our team is comprised of motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.

About Us

We are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Our mission is to transform drug and device development for partners and patients across the globe.

The Role

This role is for upcoming future opportunities that may arise at Phiture. As a Clinical Monitoring Specialist, you will be responsible for site management responsibility for clinical studies according to our Standard Operating Procedures, ICH GCP Guidelines, applicable project plans, and Sponsor requirements.

Your Key Responsibilities:

  • Conducts site monitoring responsibilities for clinical trials according to our Standard Operating Procedures (SOPs), ICH guidelines, and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.


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